Canonical Allele Identifier: CA2399818057
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750864C= , CM000684.2:g.27750864C= GRCh38
NC_000022.10:g.28146852C= , CM000684.1:g.28146852C= GRCh37
NC_000022.9:g.26476852C= NCBI36
NG_023258.1:g.55635G=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.539G=
ENST00000302326.5:c.*51G= MANE Select ENSP00000304956.4:n.*51G=
ENST00000302326.4:c.*51G= ENSP00000304956.4:n.*51G=
ENST00000424656.1:c.367G=
ENST00000497225.1:n.370G=
NM_002430.2:c.*51G= NP_002421.3:n.*51G=
NM_002430.3:c.*51G= MANE Select NP_002421.3:n.*51G=